Variant report

Variant	rs73816856
Chromosome Location	chr4:55816297-55816298
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10027862	1.00[AMR][1000 genomes]
rs11930183	1.00[AMR][1000 genomes]
rs1380070	1.00[AMR][1000 genomes]
rs1497481	1.00[AMR][1000 genomes]
rs1543930	1.00[AMR][1000 genomes]
rs1543931	1.00[AMR][1000 genomes]
rs1551639	1.00[AMR][1000 genomes]
rs17085066	1.00[AMR][1000 genomes]
rs1870380	1.00[AMR][1000 genomes]
rs4352535	1.00[AMR][1000 genomes]
rs57190330	1.00[AMR][1000 genomes]
rs59384774	1.00[AMR][1000 genomes]
rs60067051	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6824124	1.00[AMR][1000 genomes]
rs6826761	1.00[AMR][1000 genomes]
rs6835605	1.00[AMR][1000 genomes]
rs73816854	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73816855	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73818439	1.00[AMR][1000 genomes]
rs7666097	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv526344	chr4:55522488-56231119	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
2	nsv948758	chr4:55748430-55887962	Enhancers Flanking Active TSS Active TSS Weak transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:55811800-55819200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr4:55816000-55817200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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